Effect of Photofrin-mediated photocytotoxicity on a panel of human pancreatic cancer cells.
Effect of Photofrin-mediated photocytotoxicity on a panel of human pancreatic cancer cells.
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DOI:
10.1016/j.pdpdt.2012.11.001
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发表时间:
2013-09
影响因子:
3.3
通讯作者:
Liu, Bolin
中科院分区:
文献类型:
--
作者:
Wang, Luo-Wei;Huang, Zheng;Lin, Han;Li, Zhao-Shen;Hetzel, Fred;Liu, Bolin
Pancreatic cancer is a leading cause of cancer-related deaths in men and women. Early clinical studies suggest that photodynamic therapy (PDT) might be a useful modality in the management of this deadly disease. In this study, the photocytotoxicity of Photofrin-mediated PDT on different human pancreatic cancer cells (BxPc-3, HPAF-II, Mia PaCa-2, MPanc-96, PANC-1 and PL-45) was examined. After co-incubating cancer cells with Photofrin (0—10 [H9262]g/ml) for 4 h, the cells were irradiated with 0—6 J/cm2 of 630 nm light. The effect of Photofrin PDT on the survival of cells were examined using tetrazolium-based colorimetric assay and clonogenic assay. PDT-induced apoptosis was analyzed by flow cytometry. Expressions of apoptosis-related proteins were determined by western blot analysis. Photofrin PDT strongly inhibited the survival of pancreatic cancer cells. A small portion of cells (<15%) underwent apoptosis 24 h after PDT at LD50. Cleavage of caspase-3, caspase-8, caspase-9 and PARP after PDT were also confirmed. BxPc-3, Mia PaCa-2, MPanc-96, and PANC-1 cells were more sensitive and HPAF-II and PL-45 cells less sensitive. Photofrin PDT can induce apoptosis and inhibit survival of human pancreatic cancer cells.
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